Light and electron microscopy of embryo development in perennial and annual Medicago species

Abstract
The embryo of perennial Medicago sativa L. and annual M. scutellata (L.) Mill. have similar growth stages, but the perennial embryo is smaller and its rate of growth is slower than that of the annual by about 3 days. Transfer cells in the suspensor and embryo sac of late heart stages suggest different major pathways of nutrient flow in the two species. Transfusion tissue at the base of the embryo sac in the ovule of M. scutellata may facilitate solute transport and promote rapid embryo growth. Plastids in the suspensor cells of heart and late heart stages of the two species contain a dense matrix, membrane-bounded plastid vacuoles, starch, and a dense core. The plastid core in M. sativa has stacked tiers of straight tubules about 24 nm in diameter, suggesting that these specialized plastids are like tubular chromoplasts. Plastid vacuoles arise from the periphery of dense cores and apparently discharge electron-translucent contents into the suspensor cytoplasm. Plastid vacuoles may play a role in suspensor metabolism and thus influence embryo development.

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